FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term cone-rod dystrophy 10 ID (Ontology) DOID:0111017 (Human Disease)
Definition A cone-rod dystrophy that has_material_basis_in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22.
Also Known As "CORD10"
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DO.org
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 Genes
 cone-rod dystrophy 10       5
 for disease ribbon | cone-rod dystrophy 10       5
 model of | cone-rod dystrophy 10       5
Spanning Tree (Parents/Children)
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monogenic disease_____
retinal degeneration__|
                      cone-rod dystrophy
                       |__cone-rod dystrophy 10  5 rec.
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Is a cone-rod dystrophy
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Synonyms
  • "CORD10" EXACT OMO:0003012
Secondary IDs
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MESH:C564597
MIM:610283